Evidence map›Paper›PMID 30672601›Full record

ArticleHepatology (Baltimore, Md.)2019

A Large-Scale Multicenter Study Validates Aldo-Keto Reductase Family 1 Member B10 as a Prevalent Serum Marker for Detection of Hepatocellular Carcinoma.

Xu Ye, Cunyan Li, Xuyu Zu, Minglin Lin, Qiang Liu, Jianghua Liu, Guoguo Xu, Zhiyong Chen, Yongliang Xu, Long Liu and 11 more

2 registry-linked trialsOpen access · hybridAbstract readMulticenter Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06272656 unknown statusnot on this mapstarted 2024, after this paper: background citation

Evaluation of AKR1B10 as a New Marker for Interventional Therapy of Hepatocellular Carcinoma

TypeobservationalSponsorHebei Medical University Third HospitalRan2024 to 2025Enrolled200ConditionsHepatocellular Carcinoma
NCT07147335 recruitingnot on this mapstarted 2025, after this paper: background citation

The Role of Serum AKR1B10 in Early Warning of Hepatocellular Carcinoma in Cirrhosis Patients ------ Risk Early Warning and Follow-up Study

Typeobservational_patient_registrySponsorThe First Affiliated Hospital of University of South ChinaRan2025 to 2028Enrolled800ConditionsCirrhosis, Hepotacellular CarcinomaArmsserum AKR1B10 levels
3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 95 citations in OpenAlex.

  1. Pooled it
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  5. AKR1B1 and AKR1B10 as Potential Prognostic Biomarkers of Endometrial Cancer.International journal of molecular sciences · 2026
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  12. A Conserved FABP5Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
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  18. Review
  19. Biomarker in Hepatocellular Carcinoma.Indian journal of surgical oncology · 2024
    Review
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 6 institutions in 1 country.

Xu YeHunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan, China.
Cunyan LiDepartment of Laboratory Medicine, Hunan Provincial People's Hospital/the First Affiliated Hospital of Hunan Normal University, Hunan, China.
Xuyu ZuInstitute of Clinical Medicine, the First Affiliated Hospital of University of South China, Hunan, China.
Minglin LinLaboratory of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Guilin Medical University, Guangxi, China.
Qiang LiuHunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan, China.
Jianghua LiuInstitute of Clinical Medicine, the First Affiliated Hospital of University of South China, Hunan, China.
Guoguo XuLight of Life Biotechnology Co., Ltd., Hunan, China.
Zhiyong ChenLight of Life Biotechnology Co., Ltd., Hunan, China.
Yongliang XuLight of Life Biotechnology Co., Ltd., Hunan, China.
Long LiuLight of Life Biotechnology Co., Ltd., Hunan, China.
Diteng LuoLaboratory of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Guilin Medical University, Guangxi, China.
Zhe CaoLight of Life Biotechnology Co., Ltd., Hunan, China.
Guiyuan ShiLight of Life Biotechnology Co., Ltd., Hunan, China.
Zirui FengDivision of Stem Cell Regulation and Application, State Key Laboratory of Chinese Medicine Powder and Medicine Innovation in Hunan (incubation), Hunan University of Chinese Medicine, Hunan, China.
Hongyu DengHunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan, China.
Qianjin LiaoHunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan, China.
Chuan CaiDivision of Stem Cell Regulation and Application, State Key Laboratory of Chinese Medicine Powder and Medicine Innovation in Hunan (incubation), Hunan University of Chinese Medicine, Hunan, China.
Duan-Fang LiaoDivision of Stem Cell Regulation and Application, State Key Laboratory of Chinese Medicine Powder and Medicine Innovation in Hunan (incubation), Hunan University of Chinese Medicine, Hunan, China.
Jing WangHunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan, China.
Junfei JinLaboratory of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Guilin Medical University, Guangxi, China.
Deliang CaoHunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan, China.
Hunan Cancer Hospital · CNGuilin Medical University · CNHunan University of Traditional Chinese Medicine · CNCentral South University · CNFirst Affiliated Hospital of University of South China · CNHunan Normal University · CN

Funding

High Level of Innovation Team and Outstanding Scholars Program in Colleges and Universities in GuangxiLijiang Scholar Award in GuilinNational Natural Science Foundation of China 81360309National Natural Science Foundation of China 81472465National Natural Science Foundation of China 81572738National Natural Science Foundation of China 81670268National Natural Science Foundation of China 81772842Natural Science Foundation of Guangxi Province 2015GXNSFEA139003
6 · The paper itself

Abstract

Aldo-keto reductase family 1 member B10 (AKR1B10) is a secretory protein overexpressed in hepatocellular carcinoma (HCC). We aimed to evaluate AKR1B10 as a serum marker for detection of HCC. Herein, we conducted a cohort study that consecutively enrolled 1,244 participants from three independent hospitals, including HCC, healthy controls (HCs), benign liver tumors (BLTs), chronic hepatitis B (CHB), and liver cirrhosis (LC). Serum AKR1B10 was tested by time-resolved fluorescent assays. Data were plotted for receiver operating characteristic (ROC) curve analyses. Alpha-fetoprotein (AFP) was analyzed for comparison. An exploratory discovery cohort demonstrated that serum AKR1B10 increased in patients with HCC (1,567.3 ± 292.6 pg/mL; n = 69) compared with HCs (85.7 ± 10.9 pg/mL; n = 66; P < 0.0001). A training cohort of 519 participants yielded an optimal diagnostic cutoff of serum AKR1B10 at 267.9 pg/mL. When ROC curve was plotted for HCC versus all controls (HC + BLT + CHB + LC), serum AKR1B10 had diagnostic parameters of the area under the curve (AUC) 0.896, sensitivity 72.7%, and specificity 95.7%, which were better than AFP with AUC 0.816, sensitivity 65.1%, and specificity 88.9%. Impressively, AKR1B10 showed promising diagnostic potential in early-stage HCC and AFP-negative HCC. Combination of AKR1B10 with AFP increased diagnostic accuracy for HCC compared with AKR1B10 or AFP alone. A validation cohort of 522 participants confirmed these findings. An independent cohort of 68 patients with HCC who were followed up showed that serum AKR1B10 dramatically decreased 1 day after operation and was nearly back to normal 3 days after operation. Conclusion: AKR1B10 is a potent serum marker for detection of HCC and early-stage HCC, with better diagnostic performance than AFP.

Indexed as

AdultAldo-Keto Reductase Family 1 member B10Biomarkers, TumorBiopsy, NeedleCarcinoma, HepatocellularCase-Control StudiesChinaFemaleHospitals, UniversityHumansImmunohistochemistryLiver NeoplasmsMaleMiddle AgedReference ValuesReproducibility of ResultsAldo-Keto Reductase Family 1 member B10Biomarkers, Tumor

Identifiers

PMID30672601
PMCPMC6593451
OpenAlexW2912064798

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.